I am Doctor Mahmoud Gaballa, myeloma pecialist at MD Anderson Cancer Center. So my research, in this abstract, was about the use of bispecific antibodies in patients with myeloma that affects the brain. We will abbreviate that by calling it CNS myeloma, and by the brain, it's primarily the brain. But also our study included the brain, the spinal cord, and the covering around the spinal cord. So all of those represented what we call CNS myeloma.
It's a rare entity. But because we access through the consortium, which includes many academic US centers, we were able to include about 24 patients. And the systemic responses with this use was about 63%. And the CNS response was about 58%.
The duration of response, so those who responded, the duration of response, like how long it lasted, was actually unreached, which is reassuring. So once you see what is achieved response, the median duration is unreached. Median PFS was about five months, basically how long it took before the disease progresses. And so that was five months. And the median overall survival was about 12.2 months, or roughly about a year. And the manner of progression afterwards was a mixture between either CNS progression or systemic progression.
And those numbers of efficacy I just stated are a little bit worse than with the use of Car-T in CNS myeloma, which argues that perhaps trying to combine both modalities, trying to use perhaps bispecific antibodies as a bridge to Car-T, maybe that's one thing to be considered.
The other thing that we looked at is safety. One particular thing is ICANS because one particular concern is if you have a CNS myeloma that you would be concerned maybe there'll be excess ICANS. But we did not find that. We did not find any excess ICANS. The ICANS rates were about the usual of what you would expect with these products, which is encouraging.
So it basically tells physicians that you can use bispecific antibodies in patients with CNS myeloma without the fear of excessive side effects.
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